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An orthologous gene coevolution network provides insight into eukaryotic cellular and genomic structure and function
The evolutionary rates of functionally related genes often covary. We present a gene coevolution network inferred from examining nearly 3 million orthologous gene pairs from 332 budding yeast species spanning ~400 million years of evolution. Network modules provide insight into cellular and genomic...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9067921/ https://www.ncbi.nlm.nih.gov/pubmed/35507651 http://dx.doi.org/10.1126/sciadv.abn0105 |
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author | Steenwyk, Jacob L. Phillips, Megan A. Yang, Feng Date, Swapneeta S. Graham, Todd R. Berman, Judith Hittinger, Chris Todd Rokas, Antonis |
author_facet | Steenwyk, Jacob L. Phillips, Megan A. Yang, Feng Date, Swapneeta S. Graham, Todd R. Berman, Judith Hittinger, Chris Todd Rokas, Antonis |
author_sort | Steenwyk, Jacob L. |
collection | PubMed |
description | The evolutionary rates of functionally related genes often covary. We present a gene coevolution network inferred from examining nearly 3 million orthologous gene pairs from 332 budding yeast species spanning ~400 million years of evolution. Network modules provide insight into cellular and genomic structure and function. Examination of the phenotypic impact of network perturbation using deletion mutant data from the baker’s yeast Saccharomyces cerevisiae, which were obtained from previously published studies, suggests that fitness in diverse environments is affected by orthologous gene neighborhood and connectivity. Mapping the network onto the chromosomes of S. cerevisiae and Candida albicans revealed that coevolving orthologous genes are not physically clustered in either species; rather, they are often located on different chromosomes or far apart on the same chromosome. The coevolution network captures the hierarchy of cellular structure and function, provides a roadmap for genotype-to-phenotype discovery, and portrays the genome as a linked ensemble of genes. |
format | Online Article Text |
id | pubmed-9067921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-90679212022-05-13 An orthologous gene coevolution network provides insight into eukaryotic cellular and genomic structure and function Steenwyk, Jacob L. Phillips, Megan A. Yang, Feng Date, Swapneeta S. Graham, Todd R. Berman, Judith Hittinger, Chris Todd Rokas, Antonis Sci Adv Biomedicine and Life Sciences The evolutionary rates of functionally related genes often covary. We present a gene coevolution network inferred from examining nearly 3 million orthologous gene pairs from 332 budding yeast species spanning ~400 million years of evolution. Network modules provide insight into cellular and genomic structure and function. Examination of the phenotypic impact of network perturbation using deletion mutant data from the baker’s yeast Saccharomyces cerevisiae, which were obtained from previously published studies, suggests that fitness in diverse environments is affected by orthologous gene neighborhood and connectivity. Mapping the network onto the chromosomes of S. cerevisiae and Candida albicans revealed that coevolving orthologous genes are not physically clustered in either species; rather, they are often located on different chromosomes or far apart on the same chromosome. The coevolution network captures the hierarchy of cellular structure and function, provides a roadmap for genotype-to-phenotype discovery, and portrays the genome as a linked ensemble of genes. American Association for the Advancement of Science 2022-05-04 /pmc/articles/PMC9067921/ /pubmed/35507651 http://dx.doi.org/10.1126/sciadv.abn0105 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Steenwyk, Jacob L. Phillips, Megan A. Yang, Feng Date, Swapneeta S. Graham, Todd R. Berman, Judith Hittinger, Chris Todd Rokas, Antonis An orthologous gene coevolution network provides insight into eukaryotic cellular and genomic structure and function |
title | An orthologous gene coevolution network provides insight into eukaryotic cellular and genomic structure and function |
title_full | An orthologous gene coevolution network provides insight into eukaryotic cellular and genomic structure and function |
title_fullStr | An orthologous gene coevolution network provides insight into eukaryotic cellular and genomic structure and function |
title_full_unstemmed | An orthologous gene coevolution network provides insight into eukaryotic cellular and genomic structure and function |
title_short | An orthologous gene coevolution network provides insight into eukaryotic cellular and genomic structure and function |
title_sort | orthologous gene coevolution network provides insight into eukaryotic cellular and genomic structure and function |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9067921/ https://www.ncbi.nlm.nih.gov/pubmed/35507651 http://dx.doi.org/10.1126/sciadv.abn0105 |
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